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Gonosome mosaicism 4 6,XY / 4 6,XX in a case of male pseudohermaphroditism with absent uterus
Š. Sršeň, M. Kacejová, K. Sapák, A. Slameňová, P. Uhrín
Medical genetics.
1973 ;
() :
179-182.
Plzeňský lékařský sborník. Supplementum.
1973 ;
(Suppl. 31) :
179-182.
Language English Country Czech Republic
Document type Case Reports
Persistent link
https://www.medvik.cz/link/bmc14058988
Digital library NLK
Source
- MeSH
- Androgens metabolism MeSH
- Biomarkers blood urine MeSH
- Cytogenetics methods trends MeSH
- Dermatoglyphics MeSH
- Child MeSH
- Adult MeSH
- Genetic Research * MeSH
- Gonadal Dysgenesis diagnosis MeSH
- Genetics, Medical methods MeSH
- Humans MeSH
- Herniorrhaphy MeSH
- 46, XX Disorders of Sex Development * diagnosis etiology genetics MeSH
- Pedigree MeSH
- Gonadal Dysgenesis, Mixed diagnosis MeSH
- Statistics as Topic MeSH
- Uterus abnormalities pathology MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Case Reports MeSH
Department of Pediatrics and Department of Internal Medicine Martin
Research Laboratory of Clinical Genetics Komenský University Medical School Martin
University Hospital Department of Gynaecoloby and Obstetrics
Bibliography, etc.
Literatura
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